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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol | Gene ID ▼ | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C1378703 | Renal carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0003850 | Arteriosclerosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1838244 | TIBIAL MUSCULAR DYSTROPHY, TARDIVE | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C4552000 | Episodic Kinesigenic Dyskinesia 1 | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0004153 | Atherosclerosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0019569 | Hirschsprung Disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0022680 | Polycystic Kidney Diseases | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0005587 | Depression, Bipolar | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0024299 | Lymphoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0795907 | CONOTRUNCAL ANOMALY FACE SYNDROME | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0020626 | Hypoparathyroidism | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C3160718 | PARKINSON DISEASE, LATE-ONSET | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0010054 | Coronary Arteriosclerosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0026269 | Mitral Valve Stenosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0032914 | Pre-Eclampsia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1168401 | Squamous cell carcinoma of the head and neck | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0034150 | Purpura | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0029408 | Degenerative polyarthritis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0014070 | Encephalomyelitis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0036508 | Seborrheic dermatitis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0018817 | Atrial Septal Defects | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0017168 | Gastroesophageal reflux disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1704272 | Benign Prostatic Hyperplasia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0038379 | Strabismus | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0677886 | Epithelial ovarian cancer | COMT | 1312 | catechol-O-methyltransferase | P21964 |
